MONMOUTH JUNCTION, NJ--(Marketwired - Aug 7, 2013) - Insmed Incorporated (
- Matthew Pauls, Chief Commercial Officer of Insmed, will present a corporate overview at the Wedbush Pac Grow Life Sciences' 2013 Life Sciences Management Access Conference taking place from August 13-14, at Le Parker Meridian in New York City. Mr. Pauls' presentation will take place on August 13th at 2:30 p.m. Eastern time.
- Will Lewis, President and Chief Executive Officer of Insmed, will address investors at Canaccord Genuity's 33rd Annual Growth Conference taking place from August 14-15, at the Intercontinental Hotel in Boston. Mr. Lewis' presentation will be delivered on August 14th at 5:00 p.m. Eastern time.
Mr. Pauls' and Mr. Lewis' presentations will be webcast live on the internet and can be accessed by visiting the investors section of the company's website at www.insmed.com. A replay of the webcasts will be archived on the Insmed website for 90 days following the presentation.
Insmed Incorporated is a biopharmaceutical company dedicated to improving the lives of patients battling serious lung diseases. Insmed is focused on the development and commercialization of ARIKACE®, or liposomal amikacin for inhalation, for at least two identified orphan patient populations: cystic fibrosis (CF) patients with Pseudomonas aeruginosa lung infections and patients with non-tuberculous mycobacteria (NTM) lung infections. For more information, visit www.insmed.com.
This release contains forward-looking statements. Words, and variations of words, such as "intend," "expect," "will," "anticipate," "believe," "continue," "propose" and similar expressions are intended to identify forward-looking statements. Investors are cautioned that such statements in this release, including statements relating to the status, results and timing of clinical trials and clinical data, the anticipated benefits of Insmed's products, the anticipated timing of regulatory submissions, and the ability to obtain required regulatory approvals, bring products to market and successfully commercialize products constitute forward-looking statements that involve risks and uncertainties that could cause actual results to differ materially from those in the forward-looking statements. Such risks and uncertainties include, without limitation, failure or delay of European, Canadian, U.S. Food and Drug Administration and other regulatory reviews and approvals, competitive developments affecting the Company's product candidates, delays in product development or clinical trials or other studies, patent disputes and other intellectual property developments relating to the Company's product candidates, unexpected regulatory actions, delays or requests, the failure of clinical trials or other studies or results of clinical trials or other studies that do not meet expectations, the fact that subsequent analyses of clinical trial or study data may lead to different (including less favorable) interpretations of trial or study results or may identify important implications of a trial or study that are not reflected in Company's prior disclosures, and the fact that trial or study results or subsequent analyses may be subject to differing interpretations by regulatory agencies, the inability to successfully develop the Company's product candidates or receive necessary regulatory approvals, inability to make product candidates commercially successful, changes in anticipated expenses, changes in the Company's financing requirements or ability raise additional capital, and other risks and challenges detailed in the Company's filings with the U.S. Securities and Exchange Commission, including its Annual Report on Form 10-K for the year ended December 31, 2012. Investors are cautioned not to place undue reliance on any forward-looking statements that speak only as of the date of this news release. The Company undertakes no obligation to update these forward-looking statements to reflect events or circumstances or changes in its expectations.